Home> Products> Amino Acid> Special Amino Acid> L-2-Aminobutyric acid CAS NO 1492-24-6 C4H9NO2
L-2-Aminobutyric acid CAS NO 1492-24-6 C4H9NO2
L-2-Aminobutyric acid CAS NO 1492-24-6 C4H9NO2
L-2-Aminobutyric acid CAS NO 1492-24-6 C4H9NO2

L-2-Aminobutyric acid CAS NO 1492-24-6 C4H9NO2

Payment Type:L/C,T/T,D/P,D/A
Incoterm:FOB,CFR,CIF
Min. Order:1 Kilogram
Transportation:Ocean,Air
Port:Shanghai

  • Product Attributes
  • Packaging & Delivery
  • Product Description
  • Supply Ability & Additional Information
Product Attributes

BrandRonasChemical

GradeFood Grade, Medicine Grade, Reagent Grade

Packaging & Delivery
Selling Units: Kilogram
Package Type: EXPORT STANDARD PACKAGE
Product Description

PRODUCT: L (+)-2-Aminobutyric acid

CAS NO: 1492-24-6

MOLECULA FORMULA: C4H9NO2

 

MW:103.12

EINECS: 216-083-3

Product Categories: Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives; Unusual Amino Acids; Chiral Reagents; Amino Acid;Odevixibat;bc0001

Mol File: 1492-24-6.mol

 

 

PROPERTIES

LIMITS

Melting point 

300 °C

alpha 

21.6 º (c=2, 5N HCl)

Boiling point 

215.2±23.0 °C(Predicted)

density 

1.2300 (estimate)

refractive index 

1.4650 (estimate)

storage temp. 

room temp

solubility 

22.7 g/100 mL (22°C)

pka

2.29(at 25)

form 

Crystalline Powder

color 

White to beige

Water Solubility 

22.7 g/100 mL (22 ºC)

Merck 

14,428

BRN 

1720935

InChIKey

QWCKQJZIFLGMSD-VKHMYHEASA-N

 
 

L(+)-2-Aminobutyric acid Usage And Synthesis

Chemical Properties

White Crystalline Solid

Uses

aminobutyric acid is an amino acid with water-binding properties and possible anti-inflammatory capacities.

Uses

L-(+)-2-Aminobutyric acid is used in the biosynthesis of nonribosomal peptides. It acts as a receptor antagonist. It is also used as a chiral reagent. Further, it is used in the determination of substrate of glutamyl cysteine acid synthase. In addition to this, it is also utilized as a drug intermediate.

Definition

ChEBI: An optically active form of alpha-aminobutyric acid having L-configuration.

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 450, 1946 DOI: 10.1021/ja01207a032

General Description

L-2-Aminobutyric acid is synthesized from L-threonine and L-aspartic acid through a ?-transamination reaction. It is an L-alanine analogue with an ethyl side chain.

Biochem/physiol Actions

L-α-Aminobutyric acid (AABA) is an isomer of the non-natural amino acid aminobutyric acid with activity in the γ-glutamyl cycle that regulates glutathione biosynthesis. Recently AABA has been studied as a supplement to in vitro maturation medium (NCSU 23 medium) for culture of oozytes and embryos. This product has been qualified for use in cell culture. AABA is also used as a substitute amino acid for alanine in studies on peptide function.

Purification Methods

Crystallise butyrine from aqueous EtOH, and the melting point depends on heating rate but has m 303o in a sealed tube. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 p 2399 IR: 2401 1961, Beilstein 4 III 1294, 4 IV 2584.]

 
 

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Supply Ability & Additional Information

PackagingEXPORT STANDARD PACKAGE

TransportationOcean,Air

Place of OriginChina

Supply AbilityAS MUCH AS WE CAN

PortShanghai

Payment TypeL/C,T/T,D/P,D/A

IncotermFOB,CFR,CIF

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